Mellish Island Corp Recall: Firm's finished product label does not declare the source of marine collagen which was determined to be fish.
United States
OngoingClass II
- Company
- Mellish Island Corp
- Product
- Mellish Island Super Skin; Dietary Supplement; 60 Capsules,…
- Recall date
- July 1, 2026
- Source
- FDA
Reason for recall
Firm's finished product label does not declare the source of marine collagen which was determined to be fish.
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2 per day; Distributed by Mellish Island Corp. UPC: 8 58792 00332 3 | Not published in this source record | 1,600 bottles | Lot: CA1G24 Expiration: 08-2027 |
Distribution
- Product is distributed through TikTok exclusively. Presumably nationwide.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-1190-2026
- Event ID
- 99419
- Status
- Ongoing
- Classification
- Class II
- Company
- Mellish Island Corp
- Product description
- Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2 per day; Distributed by Mellish Island Corp. UPC: 8 58792 00332 3
- Quantity
- 1,600 bottles
- Reason
- Firm's finished product label does not declare the source of marine collagen which was determined to be fish.
- Recall initiation date
- July 1, 2026
- Report date
- August 5, 2026
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Product is distributed through TikTok exclusively. Presumably nationwide.
- UPC, lot, and code information
- Lot: CA1G24 Expiration: 08-2027
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Mellish Island Corp
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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